明胶
自愈水凝胶
生物相容性
自愈
肿胀 的
化学
流变学
生物材料
辣根过氧化物酶
材料科学
细胞包封
动态力学分析
化学工程
高分子化学
聚合物
纳米技术
有机化学
复合材料
酶
替代医学
病理
工程类
医学
作者
Francesca Cadamuro,Valeria Ardenti,Francesco Nicotra,Laura Russo
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2023-03-22
卷期号:28 (6): 2851-2851
被引量:17
标识
DOI:10.3390/molecules28062851
摘要
Alginate-gelatin hydrogels mimicking extracellular matrix (ECM) of soft tissues have been generated by static-dynamic double crosslinking, allowing fine control over the physical and chemical properties. Dynamic crosslinking provides self-healing and injectability attributes to the hydrogel and promotes cell migration and proliferation, while the static network improves stability. The static crosslinking was performed by enzymatic coupling of the tyrosine residues of gelatin with tyramine residues inserted in the alginate backbone, catalyzed by horseradish peroxidase (HRP). The dynamic crosslinking was obtained by functionalizing alginate with 3-aminophenylboronic acid which generates a reversible bond with the vicinal hydroxyl groups of the alginate chains. Varying the ratio of alginate and gelatin, hydrogels with different properties were obtained, and the most suitable for 3D soft tissue model development with a 2.5:1 alginate:gelatin molar ratio was selected. The selected hydrogel was characterized with a swelling test, rheology test, self-healing test and by cytotoxicity, and the formulation resulted in transparent, reproducible, varying biomaterial batch, with a fast gelation time and cell biocompatibility. It is able to modulate the loss of the inner structure stability for a longer time with respect to the formulation made with only covalent enzymatic crosslinking, and shows self-healing properties.
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